A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011487



Internal ID19100704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96380611..96472652hg38UCSC Ensembl
Innerchr4:97301762..97393803hg19UCSC Ensembl
Innerchr4:97520785..97612826hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3892042
hg1992042
hg1892042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5343n100
Supporting Variantsnssv3630986
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011487
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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